Huang J, Li Z, Yang L, Hu R, Shi G
Sci Rep. 2025; 15(1):3101.
PMID: 39856238
PMC: 11760367.
DOI: 10.1038/s41598-025-87189-z.
Amin M, Gnida P, Malecki J, Kotowicz S, Schab-Balcerzak E
Materials (Basel). 2025; 17(24.
PMID: 39769717
PMC: 11679960.
DOI: 10.3390/ma17246116.
Sharangi S, Chakraborty B, Kumar Jha R, Mandal S, Koner A, Kumar S
Chem Sci. 2024; 16(2):709-720.
PMID: 39677936
PMC: 11639539.
DOI: 10.1039/d4sc07817a.
Wolf P, Wick C, Mehler J, Blaumeiser D, Schotz S, Bauer T
ACS Catal. 2022; 12(9):5661-5672.
PMID: 35572184
PMC: 9088848.
DOI: 10.1021/acscatal.1c05979.
Bora S, Kalita D
RSC Adv. 2022; 11(62):39246-39261.
PMID: 35492466
PMC: 9044474.
DOI: 10.1039/d1ra05887h.
DFT and TD-DFT studies for optoelectronic properties of coumarin based donor-π-acceptor (D-π-A) dyes: applications in dye-sensitized solar cells (DSSCS).
Vuai S, Khalfan M, Babu N
Heliyon. 2021; 7(11):e08339.
PMID: 34816038
PMC: 8593435.
DOI: 10.1016/j.heliyon.2021.e08339.
Critical Role of Protons for Emission Quenching of Indoline Dyes in Solution and on Semiconductor Surfaces.
El-Zohry A, Agrawal S, De Angelis F, Pastore M, Zietz B
J Phys Chem C Nanomater Interfaces. 2020; 124(39):21346-21356.
PMID: 33343786
PMC: 7737328.
DOI: 10.1021/acs.jpcc.0c07099.
Dithieno[1,4]thiazines and Bis[1]benzothieno[1,4]thiazines-Organometallic Synthesis and Functionalization of Electron Density Enriched Congeners of Phenothiazine.
May L, Muller T
Molecules. 2020; 25(9).
PMID: 32392728
PMC: 7248943.
DOI: 10.3390/molecules25092180.
New Oxindole-Bridged Acceptors for Organic Sensitizers: Substitution and Performance Studies in Dye-Sensitized Solar Cells.
Tingare Y, Su C, Shen M, Tsai S, Ho S, Li W
Molecules. 2020; 25(9).
PMID: 32380749
PMC: 7248932.
DOI: 10.3390/molecules25092159.
Widely Electronically Tunable 2,6-Disubstituted Dithieno[1,4]thiazines-Electron-Rich Fluorophores Up to Intense NIR Emission.
May L, Muller T
Chemistry. 2020; 26(57):12978-12986.
PMID: 32207193
PMC: 7589349.
DOI: 10.1002/chem.202000859.
Electron-Rich Phenothiazine Congeners and Beyond: Synthesis and Electronic Properties of Isomeric Dithieno[1,4]thiazines.
May L, Muller T
Chemistry. 2020; 26(53):12111-12118.
PMID: 32017228
PMC: 7540341.
DOI: 10.1002/chem.202000137.
Effect of Auxiliary Donors on 3,8-Phenothiazine Dyes for Dye-Sensitized Solar Cells.
Buene A, Christensen M, Hoff B
Molecules. 2019; 24(24).
PMID: 31817838
PMC: 6969916.
DOI: 10.3390/molecules24244485.
New Blue Donor-Acceptor Pechmann Dyes: Synthesis, Spectroscopic, Electrochemical, and Computational Studies.
Dessi A, Sinicropi A, Mohammadpourasl S, Basosi R, Taddei M, Fabrizi de Biani F
ACS Omega. 2019; 4(4):7614-7627.
PMID: 31459854
PMC: 6648098.
DOI: 10.1021/acsomega.8b03560.
Synthesis by a Cost-Effective Method and Electroluminescence of a Novel Efficient Yellowish-Green Thermally Activated Delayed Fluorescent Molecule.
Marghad I, Kim D, Tian X, Mathevet F, Gosmini C, Ribierre J
ACS Omega. 2019; 3(2):2254-2260.
PMID: 31458527
PMC: 6641307.
DOI: 10.1021/acsomega.7b01570.
Theoretical study of the effects of modifying the structures of organic dyes based on N,N-alkylamine on their efficiencies as DSSC sensitizers.
ElKhattabi S, Hachi M, Fitri A, Benjelloun A, Benzakour M, Mcharfi M
J Mol Model. 2019; 25(1):9.
PMID: 30603796
DOI: 10.1007/s00894-018-3888-0.
Dye-Sensitized Solar Cells: Fundamentals and Current Status.
Sharma K, Sharma V, Sharma S
Nanoscale Res Lett. 2018; 13(1):381.
PMID: 30488132
PMC: 6261913.
DOI: 10.1186/s11671-018-2760-6.
Donor functionalized quinoline based organic sensitizers for dye sensitized solar cell (DSSC) applications: DFT and TD-DFT investigations.
Pounraj P, Mohankumar V, Senthil Pandian M, Ramasamy P
J Mol Model. 2018; 24(12):343.
PMID: 30470959
DOI: 10.1007/s00894-018-3872-8.
Optical and Photovoltaic Properties of Thieno[3,2-]thiophene-Based Push-Pull Organic Dyes with Different Anchoring Groups for Dye-Sensitized Solar Cells.
Fernandes S, Castro M, Pereira A, Mendes A, Serpa C, Pina J
ACS Omega. 2018; 2(12):9268-9279.
PMID: 29302638
PMC: 5748282.
DOI: 10.1021/acsomega.7b01195.
Crystallisation-enhanced bulk hole mobility in phenothiazine-based organic semiconductors.
Shinde D, Salunke J, Candeias N, Tinti F, Gazzano M, Wadgaonkar P
Sci Rep. 2017; 7:46268.
PMID: 28401918
PMC: 5388875.
DOI: 10.1038/srep46268.
Organocatalyzed Atom Transfer Radical Polymerization: Perspectives on Catalyst Design and Performance.
Theriot J, McCarthy B, Lim C, Miyake G
Macromol Rapid Commun. 2017; 38(13).
PMID: 28370656
PMC: 5496779.
DOI: 10.1002/marc.201700040.
